Job Description:We are seeking an experienced GxP Systems Engineer to support the design, deployment, integration, and management of Digital Quality Automation Systems and laboratory instrumentation within GMP-regulated environments. The ideal candidate will have strong experience working with laboratory automation systems, analytical instruments, system integrations, validation, and GxP compliance. Key Responsibilities:Support implementation, optimization, maintenance, and upgrades of Digital Q

Job Summary: We are seeking an experienced GxP System Engineer with strong expertise in Hamilton Instrumentation, laboratory automation systems, and Computer System Validation (CSV) within a regulated pharmaceutical environment. The ideal candidate will support validation, compliance, qualification, and operational activities for critical laboratory systems while ensuring adherence to FDA regulations, GxP guidelines, and data integrity standards. The candidate should possess hands-on experience

Roles& Responsibilities: Provide technical operational support for laboratory-based systems to ensure scientists can perform daily activities efficiently Build, configure, and validate laboratory IT systems and instruments, ensuring proper integration across applications such as LIMs, ELN, CDS, and equipment imaging systems Collaborate cross-functionally with Science, Facilities, Quality, and IT teams to deliver and support new lab technologies and infrastructure Develop basic scripts or auto

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role The Staff Engineer, Downstream Process Development is responsible for developing, characterizing, and defining purifi